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HRID 1289394作成日:2026年10月27日

Triphenylphosphine → 16-[2,3-Difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-benzyloxyhexyl)acetate

https://huagongshe.com/reaction/1289394

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2,2-Bis(6-benzyloxyhexyl)acetic acidHCID 18920839—
反応物2,3-Difluoro-4'-(16-hydroxyhexadecyl)oxybiphenylHCID 18920864—
溶媒TetrahydrofuranHCID 8028—
生成物16-[2,3-Difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-benzyloxyhexyl)acetateHCID 1892085392.1%

反応手順

First, 3.4 g of 2,2-bis(6-benzyloxyhexyl)acetic acid, 3.3 g of 2,3-difluoro-4'-[16-hydroxyhexadecyl]oxybiphenyl, 2.3 g of triphenylphosphine, and 50 ml of tetrahyrofuran were placed in a 100 ml flask. Then, 1.5 g of diethyl azodicarboxylate was added dropwise to the reaction mixture at 5° C. Thereafter, the reaction mixture was allowed to warm to room temperature and stirred for 8 hours. The reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/9) to obtain 5.9 g of 16-[2,3-difluorobiphenyl-4'-yl]oxyhexadecyl 2,2-bis(6-benzyloxyhexyl)acetate (Y: 92.1%). The compound thus obtained had a purity of 98.3% by HPLC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05750213
出典データセットuspto-grants-1998_05
ORD IDord-66fc7f0f7c094088babdf26475eba60e
出典メモuspto-grants-1998_05